Rs7536563
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7536563 |
| PheGenI | rs7536563 |
| nextbio | rs7536563 |
| hapmap | rs7536563 |
| 1000 genomes | rs7536563 |
| hgdp | rs7536563 |
| ensembl | rs7536563 |
| gopubmed | rs7536563 |
| geneview | rs7536563 |
| scholar | rs7536563 |
| rs7536563 | |
| pharmgkb | rs7536563 |
| gwascentral | rs7536563 |
| openSNP | rs7536563 |
| 23andMe | rs7536563 |
| 23andMe all | rs7536563 |
| SNP Nexus | |
| SNPshot | rs7536563 |
| SNPdbe | rs7536563 |
| MSV3d | rs7536563 |
| Gene | FAM69A |
| Chromosome | 1 |
| Orientation | plus |
| GMAF | 0.3425 |
| Position | 93349046 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | >1.12x risk | |
| (A;G) | 1.12x risk | |
| (G;G) | 0 | common |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with this allele is 1.12 (CI 1.06-1.18). [PMID 17660530]
| GET Evidence | |
|---|---|
| rs7536563 | |
| aa_change | |
| aa_change_short | |
| impact | pharmacogenetic |
| qualified_impact | Insufficiently evaluated pharmacogenetic |
| overall_frequency | 0.59375 |
| summary | |
